Job title: Pre-Clinical Research Project ManagerLocation: PYC Therapeutics Nedlands, Western AustraliaAbout PYC TherapeuticsPYC Therapeutics (ASX: PYC) is a clinical-stage biotechnology company creating a new generation of RNA therapies to change the lives of patients with genetic diseases. The Company utilises its proprietary drug delivery platform to enhance the potency of precision medicines within the rapidly growing and commercially proven RNA therapeutic class. PYC's drug development programs target monogenic diseases – the indications with the highest likelihood of success in clinical development.About The RoleWe are seeking a highly motivated and organised Pre-Clinical Research Project Manager, passionate about translating drugs to the clinic, to join our growing team. This role will play a pivotal role in overseeing pre-clinical studies from conception to completion.Responsibilities:Manage all aspects of pre-clinical studies, including timelines, deliverables and budgets.Develop and maintain strong relationships with internal and external stakeholders, including scientists, vendors, and management.Ensure clear communication and coordination between all project team members.Keep senior management and other stakeholders informed of program updates.Oversee vendor selection, contract negotiation, and performance management.Monitor study progress, identify and mitigate potential risks, and implement corrective actions as needed.Prepare and maintain comprehensive project documentation, ensuring compliance with all relevant SOPs and regulatory requirements.Stay up-to-date on current pre-clinical testing methods, research and regulatory guidelines.The Person:The successful candidate will have a strong foundation in project management in a life sciences related field along with a passion for science and keeping projects on track. You will have a strong desire and ability to work in a fast-paced, project-driven environment.Selection criteria - Essential:Bachelor's degree in science (preferred) or a related field.Minimum 3-5 years of experience in project management within the life sciences industry.Strong organisational skills with demonstrated success in delivering projects on time and within budget.Excellent verbal and written communication, interpersonal, and organisational skills.Strong analytical and problem-solving abilities.Experience with project management methodologies (e.g., Agile).Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).Experience with project management software a plus (e.g. MS Project, Smartsheet, Jira).Working knowledge of GLP principles and regulatory agencies (e.g.FDA, EPA, TGA) highly desirable.Excellent attention to detail, teamwork and maintain meticulous attention to project deadlines.Previous experience working with CROs and an understanding of clinical trial protocols (highly desirable).Applications MUST include:1. A statement addressing the selection criteria.2. The applicant's curriculum vitae3. The contact details of two current referees.Note: Only candidates with ongoing unrestricted rights to work in Australia will be considered as no sponsorship is offered for this role.
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